Literature DB >> 16505520

Patterns of metabolic progression to type 1 diabetes in the Diabetes Prevention Trial-Type 1.

Jay M Sosenko1, Jerry P Palmer, Carla J Greenbaum, Jeffrey Mahon, Catherine Cowie, Jeffrey P Krischer, H Peter Chase, Neil H White, Bruce Buckingham, Kevan C Herold, David Cuthbertson, Jay S Skyler.   

Abstract

OBJECTIVE: There is little information regarding the pattern of metabolic deterioration before the onset of type 1 diabetes. The goal of this study was to utilize data from the Diabetes Prevention Trial-Type 1 (DPT-1) to obtain a picture of the metabolic progression to type 1 diabetes over a period of approximately 2.5 years before its diagnosis. RESEARCH DESIGN AND METHODS: Fifty-four DPT-1 participants (22 in the parenteral trial and 32 in the oral trial) were studied. All had oral glucose tolerance tests (OGTTs) at 6-month intervals from approximately 30 to 6 months before diagnosis. The vast majority also had OGTTs at diagnosis. Changes in OGTT glucose and C-peptide indexes from 30 to 6 months before diagnosis were examined by calculating slopes of the indexes for each individual over that time period. Changes from 6 months before diagnosis to diagnosis were examined by paired comparisons of the OGTT metabolic indexes between the time points.
RESULTS: Glucose levels increased gradually from 30 to 6 months before diagnosis in both the parenteral and oral groups (P < 0.001 for all indexes). Area under the curve (AUC) C-peptide (P < 0.05) and AUC C-peptide-to-AUC glucose ratio (P < 0.001) values decreased in the oral group; peak C-peptide-to-2-h glucose ratio values decreased in both groups (P < 0.001). In participants who also had OGTTs at diagnosis, AUC C-peptide (parenteral group, P < 0.05) and peak C-peptide (oral group, P < 0.05) values decreased from the last 6 months before diagnosis; stimulated C-peptide-to-glucose ratio values decreased in both groups (P < 0.001). Conversely, fasting C-peptide levels increased in both groups (oral group, P < 0.01). Fasting C-peptide-to-fasting glucose ratio values remained constant throughout the 30-month follow-up.
CONCLUSIONS: These data indicate that over a period of at least 2 years, glucose tolerance gradually deteriorates as stimulated C-peptide levels slowly decline in a substantial number of individuals who develop type 1 diabetes. However, fasting C-peptide levels are maintained, even at diagnosis.

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Year:  2006        PMID: 16505520     DOI: 10.2337/diacare.29.03.06.dc05-1006

Source DB:  PubMed          Journal:  Diabetes Care        ISSN: 0149-5992            Impact factor:   19.112


  63 in total

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2.  The role of proteomics in assessing beta-cell dysfunction and death in type 1 diabetes.

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4.  β cell death and dysfunction during type 1 diabetes development in at-risk individuals.

Authors:  Kevan C Herold; Sahar Usmani-Brown; Tara Ghazi; Jasmin Lebastchi; Craig A Beam; Melena D Bellin; Michel Ledizet; Jay M Sosenko; Jeffrey P Krischer; Jerry P Palmer
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Review 5.  Immunomodulatory therapy to preserve pancreatic β-cell function in type 1 diabetes.

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8.  Progression to diabetes in relatives of type 1 diabetic patients: mechanisms and mode of onset.

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9.  Diabetic subjects diagnosed through the Diabetes Prevention Trial-Type 1 (DPT-1) are often asymptomatic with normal A1C at diabetes onset.

Authors:  Taylor M Triolo; H Peter Chase; Jennifer M Barker
Journal:  Diabetes Care       Date:  2009-05       Impact factor: 17.152

10.  Incident dysglycemia and progression to type 1 diabetes among participants in the Diabetes Prevention Trial-Type 1.

Authors:  Jay M Sosenko; Jerry P Palmer; Lisa Rafkin-Mervis; Jeffrey P Krischer; David Cuthbertson; Jeffery Mahon; Carla J Greenbaum; Catherine C Cowie; Jay S Skyler
Journal:  Diabetes Care       Date:  2009-06-01       Impact factor: 19.112

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